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Alternatively, direct upload your vcf to MegaQuery of VarioWatch (http://genepipe.ncgm.sinica.edu.tw/v...n.do?mega=true) should receive your results online in real time.
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You might also want to try www.gene-talk.de . It is an wiki-like expert platform for filtering and annotating sequence variants. The automatic annotation is based on annovar. For the interpreation of unkown variants other expert users might assist you,...
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Thank you for this wonderful suggestion. ANNOVAR is great!Originally posted by ulz_peter View Posttry annovar:
http://www.openbioinformatics.org/annovar/
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Thanks ulz_peter, I am looking into this now.Originally posted by ulz_peter View Posttry annovar:
http://www.openbioinformatics.org/annovar/
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The problem is the shortcut in their folders are not working on the above mentioned ftp site.Originally posted by genomicist View PostMaybe, try this one:
ftp://gatk-ftp:[email protected]/refGene/
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Annotating VCF files
Can anybody tell me how to annotate vcf files for hg19 aligned file? I tried GATK, vcftools and vcfCodingSnps.
GATK - I couldn't find their refGene file in their ftp server
ftp://gatk-ftp:[email protected]
vcftools: I am having a hard time running it - it gives me "tabix" error
vcfCodingSnps: I was not able to compile on my mac - OS X 10.6, 64 bit
It will be great if anybody can give me a complied code for this architecture.
Thanks.Tags: None
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